Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | DNM2 CL E G H | 1785 | 2974 | OMIM:160150 | Myopathy, centronuclear, autosomal dominant | | | | 167 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | EMD CL E G H | 2010 | 3331 | ORPHA:98863 | X-linked Emery-Dreifuss muscular dystrophy | | | | 107 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | FHL1 CL E G H | 2273 | 3702 | ORPHA:98863 | X-linked Emery-Dreifuss muscular dystrophy | | | | 68 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | HNRNPDL CL E G H | 9987 | 5037 | OMIM:609115 | Limb-girdle muscular dystrophy, type 1G | | | | 5 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | LMNA CL E G H | 4000 | 6636 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | | | | 645 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | LMNA CL E G H | 4000 | 6636 | ORPHA:98855 | Autosomal recessive Emery-Dreifuss muscular dystrophy | | | | 645 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | LMX1B CL E G H | 4010 | 6654 | OMIM:161200 | Nail-Patella syndrome | | | | 165 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | MORC2 CL E G H | 22880 | 23573 | ORPHA:466768 | Autosomal dominant Charcot-Marie-Tooth disease type 2Z | | | | 8 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | MTMR14 CL E G H | 64419 | 26190 | OMIM:160150 | Myopathy, centronuclear, autosomal dominant | | | | 7 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | SGCD CL E G H | 6444 | 10807 | ORPHA:219 | Delta-sarcoglycan-related limb-girdle muscular dystrophy R6 | | | | 223 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | SYNE1 CL E G H | 23345 | 17089 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | | | | 1129 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | SYNE2 CL E G H | 23224 | 17084 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | | | | 508 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | TCAP CL E G H | 8557 | 11610 | OMIM:601954 | Muscular dystrophy, limb-girdle, type 2G | | | | 78 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | TMEM43 CL E G H | 79188 | 28472 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | | | | 171 | | |
HP:0001457 | HP:0001457 | Abnormality of the musculature of the upper arm | 0 | TRPV4 CL E G H | 59341 | 18083 | OMIM:606071 | Hereditary motor and sensory neuropathy, type IIC | | | | 214 | | |
HP:0001457 | HP:0033449 | Decreased mid-arm muscle circumference | 1 | CL E G H | | | | | | | | | | |
HP:0001457 | HP:0033448 | Increased mid-arm muscle circumference | 1 | CL E G H | | | | | | | | | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | DNM2 CL E G H | 1785 | 2974 | OMIM:160150 | Myopathy, centronuclear, autosomal dominant | | | | 167 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | EMD CL E G H | 2010 | 3331 | ORPHA:98863 | X-linked Emery-Dreifuss muscular dystrophy | HP:0040282 - Frequent | | | 107 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | FHL1 CL E G H | 2273 | 3702 | ORPHA:98863 | X-linked Emery-Dreifuss muscular dystrophy | HP:0040282 - Frequent | | | 68 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | HNRNPDL CL E G H | 9987 | 5037 | OMIM:609115 | Limb-girdle muscular dystrophy, type 1G | . | | | 5 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | LMNA CL E G H | 4000 | 6636 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | HP:0040282 - Frequent | | | 645 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | LMNA CL E G H | 4000 | 6636 | ORPHA:98855 | Autosomal recessive Emery-Dreifuss muscular dystrophy | HP:0040282 - Frequent | | | 645 | | |
HP:0001457 | HP:0001468 | Aplasia/Hypoplasia involving the musculature of the upper arm | 1 | LMX1B CL E G H | 4010 | 6654 | OMIM:161200 | Nail-Patella syndrome | | | | 165 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | MORC2 CL E G H | 22880 | 23573 | ORPHA:466768 | Autosomal dominant Charcot-Marie-Tooth disease type 2Z | HP:0040282 - Frequent | | | 8 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | MTMR14 CL E G H | 64419 | 26190 | OMIM:160150 | Myopathy, centronuclear, autosomal dominant | | | | 7 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | SGCD CL E G H | 6444 | 10807 | ORPHA:219 | Delta-sarcoglycan-related limb-girdle muscular dystrophy R6 | HP:0040282 - Frequent | | | 223 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | SYNE1 CL E G H | 23345 | 17089 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | HP:0040282 - Frequent | | | 1129 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | SYNE2 CL E G H | 23224 | 17084 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | HP:0040282 - Frequent | | | 508 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | TCAP CL E G H | 8557 | 11610 | OMIM:601954 | Muscular dystrophy, limb-girdle, type 2G | . | | | 78 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | TMEM43 CL E G H | 79188 | 28472 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | HP:0040282 - Frequent | | | 171 | | |
HP:0001457 | HP:0008948 | Proximal upper limb amyotrophy | 1 | TRPV4 CL E G H | 59341 | 18083 | OMIM:606071 | Hereditary motor and sensory neuropathy, type IIC | | | | 214 | | |
HP:0001457 | HP:0009784 | Aplasia/Hypoplasia of the triceps | 2 | LMX1B CL E G H | 4010 | 6654 | OMIM:161200 | Nail-Patella syndrome | | | | 165 | | |
HP:0001457 | HP:0009782 | Aplasia/Hypoplasia of the biceps | 2 | LMX1B CL E G H | 4010 | 6654 | OMIM:161200 | Nail-Patella syndrome | | | | 165 | | |
HP:0001457 | HP:0100855 | Triceps hypoplasia | 3 | CL E G H | | | | | | | | | | |
HP:0001457 | HP:0009007 | Biceps hypoplasia | 3 | CL E G H | | | | | | | | | | |
HP:0001457 | HP:0009783 | Biceps aplasia | 3 | LMX1B CL E G H | 4010 | 6654 | OMIM:161200 | Nail-Patella syndrome | . | | | 165 | | |
HP:0001457 | HP:0009785 | Triceps aplasia | 3 | LMX1B CL E G H | 4010 | 6654 | OMIM:161200 | Nail-Patella syndrome | . | | | 165 | | |